Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.



Job Description

In this role, you will build focus on line management and mentoring of Monitors on project-specific activities.


Hybrid workstyle at either Tokyo or Osaka office.


The scope of responsibilities will include:



  • Prepare, conduct and report site selection, initiation, routine monitoring and closeout visits.

  • Act as a Mentor for the Monitors on project-specific activities and supporting their professional development.

  • Plan and conduct supervised monitoring visits with training, authorization, and ongoing assessment purposes.

  • Build and maintain good relationships with sites’ staff involved in the study conduct.

  • Contribute to the performance appraisal of monitors.

  • Training, coaching and mentoring the Clinical Operations team.

  • Supervise activities of Site Management Associates related to the flow of documents and laboratory supplies between the site and the Central/Regional Laboratory/Central Reviewer.

  • Development and implementation of quality control, ensuring data integrity and compliance at a site level.

  • Ensure proper handling, accountability and reconciliation of all Investigational Products and clinical study supplies.

  • Supports Clinical Operations Managers with resource allocation and
    utilization of departmental staff

  • Performs additional Clinical Operations supervisory tasks at the discretion of
    their Line Manager



Qualifications

Qualifications


College/University degree in Life Sciences or an equivalent combination of education, training & experience.



  • Minimum 2 years of CRA mentoring or training experience.

  • Full working proficiency in Japanese and English.

  • Ability to successfully mentor and train Clinical Operations staff.

  • Proficiency in MS Office applications.

  • Availability to travel (up to 60%).

  • Ability to plan and work in a dynamic team environment.

  • Communication, collaboration, and problem-solving skills.



Additional Information

Make the right call and take your career to a whole new level.  Join the company that focuses on its people and invests in their professional development and success.

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Clinical Operations Lead (Tokyo or Osaka)

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